Services We Offer

  • CFR 21, Part 11 Consulting
  • Validation Project Management
  • Calibration Program Development
  • Software Design and Validation
  • Utility systems Validation
  • Equipment Validation
  • Validation Master Plan Development

About Control Quest

Control Quest provides Pharmaceutical and Biotechnology industries with Enterprise solutions designed specifically to meet the stringent demands of cGMP Regulations. Whether you need consulting in validation services or developing of Enterprise software applications, Control Quest can do it for you.

Our Product

Electronic Log Book allows users to maintain equipment and software modifications while offering compliance capabilities. Users can record, manage and track changes in records associated with processes, equipment, and software. CQI provides both Event and Data Logs for our clients. Event logs trace changes in software, equipment alterations, and other more general evants. Whereas Data Logs track specific process parameters.